InvaTech Pharma Solutions LLC

FDA inspection history in East Brunswick, New Jersey, 2017 to 2023

4
Form 483s

Every document, by year

  • Form 483

2017: two Form 483s; 2019: one Form 483; 2023: one Form 483.

The story so far

Built from the dates and citations on the documents themselves.

  1. 2017–19Three Form 483s, at East Brunswick, New Jersey.
  2. 2023One Form 483, at East Brunswick, New Jersey.
  3. 2023The longest 483 on file: 8 observations over 10 pages at East Brunswick, New Jersey.

Cited most

Across all InvaTech Pharma Solutions observations on file

The complete InvaTech Pharma Solutions file.

All 4 documents as original PDFs, in one order. For supplier audits, diligence and inspection prep.

$396

The price of the documents, added to your cart together

Sites

Documents

4 on file, newest first
DateDocumentPrice
2023-06-09483 Form 483$99
2019-02-07483 Form 483$99
2017-12-28483 Form 483$99
2017-04-04483 Form 483$99

FEI number 3009964119 · most recent document Jun 9, 2023

About InvaTech Pharma Solutions LLC

How many FDA Form 483s has InvaTech Pharma Solutions LLC received?

FDA Intel has 4 Form 483s on file for InvaTech Pharma Solutions LLC; the most recent is dated Jun 9, 2023.

When was InvaTech Pharma Solutions LLC last inspected by FDA?

The most recent FDA inspection document on file for InvaTech Pharma Solutions LLC is a Form 483 dated Jun 9, 2023, for the site in East Brunswick, New Jersey.

What did FDA cite at InvaTech Pharma Solutions LLC?

The regulations cited most in the observations on file for InvaTech Pharma Solutions LLC are 21 CFR 211.192 (Production record review), 3 times; 21 CFR 211.103 (Calculation of yield), 2 times; 21 CFR 211.160 (General requirements), 2 times.

InvaTech Pharma Solutions LLC FDA Inspection History & 483s · FDA Intel